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作 者:白秀英[1] 俞文华[1] 周爱儒[1] 杜国光[1]
机构地区:[1]北京医科大学生物化学与分子生物学系
出 处:《中国生物化学与分子生物学报》1999年第1期114-117,共4页Chinese Journal of Biochemistry and Molecular Biology
基 金:国家自然科学基金
摘 要:甲状旁腺素(PTH)是调节钙磷代谢的经典激素,有报道PTH对其靶细胞-成骨细胞有促增殖分化作用。经多层次、多水平的实验研究证实,PTH对成骨样细胞ROS17/2.8确有促增殖作用。(1)细胞计数、MTT[3-(4,5-dimethylthia-zol-z-yi)2,5-diphenyltetrazoliumbromide]测定及SRB(sodiumrhodamineB,SRB)染色均显示经PTH(10-9mol/L)处理的细胞,其数目明显增加;(2)3H-TdR参入增加;(3)与增殖相关的原癌基因(c-fos、c-jun、c-ki-ras和c-myc)的表达增强;(4)成骨细胞特征性蛋白-碱性磷酸酶活性降低.这些结果不仅表明该激素具有非经典样作用。Parathyroid hormone(PTH) is regarded conventionally as a regulator of homeostasis of calcium and phosphate in extracellular fluid. It has been reported recently that intermittent pulses of PTH stimulate bone formation in animals and humans. It is suggested that the anabolic effect of PTH on bone is partly due to a stimulation of osteoblast proliferation. The objectives were to determine if PTH would induce the proliferative effect on rat osteoblast like ROS 17/2.8 cells. Cells were treated with PTH (10 9 mol/L) for 8 days,the result demonstrated that cell growth could be increased by PTH treatment, 3H TdR incorporation, MTT [3 (4,5 dimethylthia zol z yi)2,5 diphenyl tetrazolium bromide] assay and SRB (sodium rhodamine B) assay were all signi ficantly enhanced as well. PTH could also induce the gene expression of proto oncogenes,c fos,c jun,c myc and c ki ras.Furthermore,the activity of alkaline phosphatase, a differential maturation marker protein of bone cells, was depressed after PTH treatment. Thus,all these findings provide further support for the anabolic effect of PTH on osteoblast like cells. However, other growth factors and/or cytokines may have synergistic action with PTH on bone cell proliferation.
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